Executive - Analytical Sciences

Roles & Responsibilities
• Develop physicochemical analytical methods within the Analytical Sciences group
• Lead and support development, qualification, and validation of physicochemical methods for batch release of monoclonal antibodies (mAbs)
• Perform structural characterization of biologics expressed in CHO or murine myeloma cell lines
• Utilize advanced analytical techniques for glycan profiling, purity, identity, and higher-order structure evaluation
• Support biosimilar development programs with robust analytical data generation
• Contribute to method transfer, documentation, and regulatory compliance activities
• Collaborate cross-functionally with manufacturing, quality, and regulatory teams
• Ensure accurate reporting and scientific documentation aligned with GMP standards

Qualification
• M.Sc in Biochemistry / Biotechnology / Life Sciences

Experience
• 1–2 years of experience in physicochemical method development and validation
• Minimum 1 year experience in biosimilar analytical development preferred
• Hands-on experience in characterization of monoclonal antibodies and related biologics

Technical Skills
• Experience with SEC-HPLC, RP-HPLC, CEX, Maurice (Capillary Electrophoresis)
• NP-HPLC for glycan characterization in mAbs
• DLS, DSC, CD Spectroscopy, SEC-MALS, and spectrophotometry-based methods
• Experience in purity and identity assessment for mAbs, bi-specific antibodies, receptor fusions, and antibody fragments
• Knowledge of higher-order structure analysis techniques
• Familiarity with Mass Spectrometry (optional but preferred)
• Working knowledge of statistical software such as GraphPad, JAMP, etc.

Core Competencies
• Strong understanding of monoclonal antibody structure and characterization
• Excellent cross-functional communication skills
• Strong analytical and problem-solving capabilities
• Effective documentation and reporting skills
• Good oral and written communication abilities

About the Company
Lambda Therapeutic Research Ltd. is expanding its Contract Development & Manufacturing Organization (CDMO) capabilities to provide integrated solutions in biologics drug development, GMP manufacturing, and First-in-Human (FIH) clinical trials, supporting global customers with end-to-end development and commercialization services.